FDA.reportPublic FDA data

NDC 50090-2007-01 - Divalproex Sodium

This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.

Product NDC
50090-2007
Requested NDC
50090-2007-01
Package NDCs from labels
50090-2007-0, 50090-2007-1, 50090-2007-01
Manufacturer
A-S Medication Solutions
Effective date
2024-04-23
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Divalproex Sodium - A-S Medication SolutionsA-S Medication Solutions2024-04-23HUMAN PRESCRIPTION DRUG LABEL

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Related label table
NDCEffectiveRelated label
50090-2007-02023-02-07These highlights do not include all the information needed to use DIVALPROEX SODIUM DELAYED-RELEASE TABLETS safely and effectively. See full prescribing information for DIVALPROEX SODIUM DELAYED-RELEASE TABLETS. DIVALPROEX SODIUM delayed-release tablets, for oral use Initial U.S. Approval: 1983
50090-2007-12023-02-07These highlights do not include all the information needed to use DIVALPROEX SODIUM DELAYED-RELEASE TABLETS safely and effectively. See full prescribing information for DIVALPROEX SODIUM DELAYED-RELEASE TABLETS. DIVALPROEX SODIUM delayed-release tablets, for oral use Initial U.S. Approval: 1983
50090-2007-02023-01-30These highlights do not include all the information needed to use DIVALPROEX SODIUM DELAYED-RELEASE TABLETS safely and effectively. See full prescribing information for DIVALPROEX SODIUM DELAYED-RELEASE TABLETS. DIVALPROEX SODIUM delayed-release tablets, for oral use Initial U.S. Approval: 1983
50090-2007-12023-01-30These highlights do not include all the information needed to use DIVALPROEX SODIUM DELAYED-RELEASE TABLETS safely and effectively. See full prescribing information for DIVALPROEX SODIUM DELAYED-RELEASE TABLETS. DIVALPROEX SODIUM delayed-release tablets, for oral use Initial U.S. Approval: 1983

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
50090-2007-0Divalproex Sodium30 in 1 BOTTLETABLET, DELAYED RELEASE3022
50090-2007-1Divalproex Sodium100 in 1 BOTTLETABLET, DELAYED RELEASE10022

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
50090-2007DIVALPROEX SODIUM TABLET, DELAYED RELEASE [A-S MEDICATION SOLUTIONS]22Current NDC, Legacy NDC, 2 package rows20240425_8ecfe765-d743-4308-9cd9-4a7b1a229ea9.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
50090-2007-0EA - Each50090-200755da1874-9b47-405d-b48c-79c1eb4dfd3b12018-12-13
50090-2007-1EA - Each50090-2007aaa8d9ba-d520-4e69-ab5d-43c9b77ed4e312021-09-07

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 56 of 325 · 6,482 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Smart Care Licensed Hand Sanitizer Hot Wheels RedALCOHOLShenzhen Lantern Scicence Co.,Ltd.4efefd07-c1df-695a-e063-6294a90a51eb2026-04-08WarningsExact identifier
unii: 3K9958V90M
Smart Care Licensed Hand Sanitizer Hot Wheels PurpleALCOHOLShenzhen Lantern Scicence Co.,Ltd.4eff601c-7bcd-1ddd-e063-6294a90a80402026-04-08WarningsExact identifier
unii: 3K9958V90M
Smart Care Hand Sanitizer Ocean BreezeALCOHOLShenzhen Lantern Scicence Co.,Ltd.4effb28e-fa83-5a06-e063-6394a90aa2f52026-04-08WarningsExact identifier
unii: 3K9958V90M
Divalproex sodiumDIVALPROEX SODIUMAlembic Pharmaceuticals Inc.fea19b14-d8ed-4954-bc54-b9240f78b3c32026-04-08Boxed warning, Warnings, Adverse reactionsExact identifier
unii: 644VL95AO6
Divalproex sodiumDIVALPROEX SODIUMPreferred Pharmaceuticals, Inc.83a77f60-ed58-4fa0-a584-e6a0c767d19d2026-04-08Boxed warning, Warnings, Adverse reactionsExact identifier
unii: 644VL95AO6
Nu Colour Bioadaptive BB Plus Foundation - Light GoldenTITANIUM DIOXIDENSE Products, Inc.faae6f47-19f3-41cb-8e0d-388569b5c73d2026-04-07WarningsExact identifier
unii: 15FIX9V2JP
Ultra SunscreenOCTINOXATE, OCTISALATE, TITANIUM DIOXIDEJiangsu Senwo Medical Technology Co., Ltd.4ed974b8-6c11-08e0-e063-6294a90a77132026-04-07WarningsExact identifier
unii: 15FIX9V2JP
XtraCare Hand Sanitizer Antibacterial Moisturize with Vitamin E and AloeALCOHOLRejoice Industries Canada Inc.28804477-c19d-4ace-93fe-a400f3bb45f12026-04-07WarningsExact identifier
unii: 3K9958V90M
70%ISOPROPYL ALCOHOLPerrigo Direct, Incf953a249-07ad-40a1-8aea-b2d419fd3d4d2026-04-07Warnings, Adverse reactionsExact identifier
unii: ND2M416302
XtraCare Hand Sanitizer Antibacterial Moisturize with Vitamin EALCOHOLRejoice Industries Canada Inc.b79d4c90-6e5c-475f-9bb3-6017a2d637932026-04-07WarningsExact identifier
unii: 3K9958V90M
B-Pure Moisturizing Hand Sanitizer Spiced Marshmallow Latte ScentedALCOHOLFourstar Group USA, Inc.38239b41-c8e1-4987-980e-b40bba5a94142026-04-07WarningsExact identifier
unii: 3K9958V90M
B-Pure Moisturizing Hand Sanitizer Creamy Vanilla and Honey ScentedALCOHOLFourstar Group USA, Inc.0225ef4f-a035-4096-9da2-44dcb902443a2026-04-07WarningsExact identifier
unii: 3K9958V90M
Neutrogena MINERAL UV TINT FACE MEDIUM DEEP SPF 30TITANIUM DIOXIDE, ZINC OXIDEAcupac Packaging, Inc4ee39bbf-b7d7-8f87-e063-6294a90a25392026-04-07WarningsExact identifier
unii: 15FIX9V2JP
H-Focus FormulaAGNUS CASTUS, AVENA SATIVA, BARYTA CARBONICA, IGNATIA AMARA, LYCOPODIUM CLAVATUM, NATRUM CARBONICUM, NATRUM MURIATICUM, PHOSPHORICUM ACIDUM, SILICEA, ZINCUM METALLICUMHealing Natural Oils LLC4ee42911-3064-7f55-e063-6294a90abcc72026-04-07WarningsExact identifier
unii: ETJ7Z6XBU4
H-Mood FormulaAGRIMONIA EUPATORIA, FLOS, ANACARDIUM ORIENTALE, AURUM METALLICUM, AVENA SATIVA, BORAGO OFFICINALIS, CAPSICUM ANNUUM, CARPINUS BETULUS, FLOS, CIMICIFUGA RACEMOSA, CINCHONA OFFICINALIS, HYPERICUM PERFORATUM, KALI BROMATUM, LARIX DECIDUA, FLOS, NATRUM CARBONICUM, NATRUM MURIATICUM, NATRUM SULPHURICUM, PHOSPHORICUM ACIDUM, PHOSPHORUS, PULSATILLA, SILICEA, SINAPSIS ARVENSIS, FLOS, TABACUMHealing Natural Oils LLC4ee5c82e-9edf-c36e-e063-6394a90a237f2026-04-07WarningsExact identifier
unii: ETJ7Z6XBU4
Nu Colour Bioadaptive BB plus Foundation - BeigeTITANIUM DIOXIDENSE Products, Inc.f74e83fe-41a0-4998-ae53-30ed5af475922026-04-07WarningsExact identifier
unii: 15FIX9V2JP
Divalproex SodiumDIVALPROEX SODIUMPreferred Pharmaceuticals Inc.d1d4d790-73d5-4a3b-a786-99f2c98125462026-04-07Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 1099678
unii: 644VL95AO6
divalproex sodiumDIVALPROEX SODIUMZydus Pharmaceuticals USA Inc.ed710c62-8ba6-4f19-b240-3ee73cd03d672026-04-06Boxed warning, Warnings, Adverse reactionsExact identifier
unii: 644VL95AO6
Divalproex SodiumDIVALPROEX SODIUMAurobindo Pharma Limiteddbd47222-14f1-4588-a009-9b81b55ca60d2026-04-06Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 1099678
rxcui: 1099870
rxcui: 1099625
unii: 644VL95AO6
CalamineCALAMINE 8%, ZINC OXIDE 8%Farmacias De Similares TX LLC4ecd0add-11c9-cf3b-e063-6394a90adff62026-04-06WarningsExact identifier
unii: 1K09F3G675

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.